Hamaguchi T, Azuma J, Awata N, Ohta H, Takihara K, Harada H, Kishimoto S, Sperelakis N
Third Department of Internal Medicine, Osaka University Medical School, Japan.
Res Commun Chem Pathol Pharmacol. 1988 Jan;59(1):21-30.
The effect of taurine on doxorubicin-induced cardiotoxicity was examined in mice. A single intraperitoneal injection of doxorubicin (15 mg/kg) produced a significant elevation of calcium and lipoperoxide content at 72 hr, as well as a significant depletion of creatine phosphokinase, glutamic oxaloacetic transaminase and lactate dehydrogenase activities at 48 hr and glutathione peroxidase activity at 24 hr in the myocardium. These results suggest that a substantial myocardial damage had occurred. All biochemical alterations except depletion of glutathione peroxidase, were markedly attenuated by the combined oral and intraperitoneal administration of taurine. Taurine significantly improved the survival rate of the mice treated with doxorubicin. These results demonstrate that taurine antagonized doxorubicin-induced cardiotoxicity.
在小鼠中研究了牛磺酸对阿霉素诱导的心脏毒性的影响。单次腹腔注射阿霉素(15毫克/千克)在72小时时导致钙和脂质过氧化物含量显著升高,以及在48小时时心肌中肌酸磷酸激酶、谷草转氨酶和乳酸脱氢酶活性显著降低,在24小时时谷胱甘肽过氧化物酶活性降低。这些结果表明已经发生了实质性的心肌损伤。除了谷胱甘肽过氧化物酶的消耗外,所有生化改变都通过口服和腹腔联合给予牛磺酸而显著减轻。牛磺酸显著提高了用阿霉素治疗的小鼠的存活率。这些结果证明牛磺酸拮抗了阿霉素诱导的心脏毒性。